The effect of carvacrol on oxido-inflammatory ovarian injury and infertility induced by ischemia-reperfusion in rats

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Özet

Background: Increased oxidants and proinflammatory cytokines play a role in the pathogenesis of ovarian ischemia-reperfusion (OIR) injury and related infertility. Carvacrol has antioxidant, antibacterial and anti-inflammatory properties. Methods: Protective effect of carvacrol against ischemia-reperfusion (IR)-related ovarian damage and infertility was investigated. IR process were applied to the ovaries of rats, which were divided into the following groups (n = 12): OIR, IR +50 mg/kg carvacrol (IRC-50), IR +100 mg/kg carvacrol (IRC-100) and sham group (SG). After the reperfusion process, six rats from each group were killed and the removed ovaries were examined biochemically and histopathologically. The remaining animals were kept two months with mature male rats to reproduce. Results: At a dose of 50 mg/kg, carvacrol suppressed the oxidant parameter increase and antioxidant decrease caused by IR in ovarian tissue. At a dose of 100 mg/kg, carvacrol antagonized both oxidant and proinflammatory cytokine increase and antioxidant decrease. Histopathologically, severe degeneration of follicles in the ovaries of the OIR group, necrotic cell accumulations, hemorrhage in the corpus luteum, edema in the interstitial tissue, polymorphous nuclear leukocyte (PNL) infiltration, and congestion and dilation of blood vessels were detected. Inflammatory symptoms such as edema in the ovarian tissue, congested dilated blood vessels and PNL infiltration were observed at a dose of 50 mg/kg of carvacrol, but these histopathological findings were not observed at a dose of 100 mg/kg. Conclusion: A dose of 100 mg/kg carvacrol, which eliminated inflammatory damage, significantly prevented the development of IR-induced infertility. Carvacrol may be beneficial in the treatment of IR-related ovarian damage and infertility. Copyright:

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https://rdlopen.rawdatalibrary.net/r/bayburt/13516Resmi atıflarda kullanılan kalıcı adres
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https://doi.org/10.31083/j.ceog4903058Yayıncı resmi DOI adresi
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2
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Tam Kayıt
AlanDeğerDil
dc.contributor.authorSahin, Nurullah
dc.contributor.authorDelibas, Ilhan Bahri
dc.contributor.authorIsaoglu, Unal
dc.contributor.authorSuleyman, Bahadir
dc.contributor.authorYazici, Gulce Naz
dc.contributor.authorCoban, Taha Abdulkadir
dc.contributor.authorUzel, Kemine
dc.contributor.authorSuleyman, Halis
dc.contributor.authorArslan, Veysel
dc.date.accessioned2026-10-29T19:11:05.196067782Z
dc.date.available2026-10-29T19:11:05.196067782Z
dc.date.issued2022
dc.description.abstractBackground: Increased oxidants and proinflammatory cytokines play a role in the pathogenesis of ovarian ischemia-reperfusion (OIR) injury and related infertility. Carvacrol has antioxidant, antibacterial and anti-inflammatory properties. Methods: Protective effect of carvacrol against ischemia-reperfusion (IR)-related ovarian damage and infertility was investigated. IR process were applied to the ovaries of rats, which were divided into the following groups (n = 12): OIR, IR +50 mg/kg carvacrol (IRC-50), IR +100 mg/kg carvacrol (IRC-100) and sham group (SG). After the reperfusion process, six rats from each group were killed and the removed ovaries were examined biochemically and histopathologically. The remaining animals were kept two months with mature male rats to reproduce. Results: At a dose of 50 mg/kg, carvacrol suppressed the oxidant parameter increase and antioxidant decrease caused by IR in ovarian tissue. At a dose of 100 mg/kg, carvacrol antagonized both oxidant and proinflammatory cytokine increase and antioxidant decrease. Histopathologically, severe degeneration of follicles in the ovaries of the OIR group, necrotic cell accumulations, hemorrhage in the corpus luteum, edema in the interstitial tissue, polymorphous nuclear leukocyte (PNL) infiltration, and congestion and dilation of blood vessels were detected. Inflammatory symptoms such as edema in the ovarian tissue, congested dilated blood vessels and PNL infiltration were observed at a dose of 50 mg/kg of carvacrol, but these histopathological findings were not observed at a dose of 100 mg/kg. Conclusion: A dose of 100 mg/kg carvacrol, which eliminated inflammatory damage, significantly prevented the development of IR-induced infertility. Carvacrol may be beneficial in the treatment of IR-related ovarian damage and infertility. Copyright:
dc.identifier.articlenumber058
dc.identifier.doi10.31083/j.ceog4903058
dc.identifier.eissn2709-0094
dc.identifier.issn0390-6663
dc.identifier.issue3
dc.identifier.scopus2-s2.0-85127470040
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/bayburt/13516
dc.identifier.volume49
dc.identifier.wosWOS:000780771900012
dc.language.isoen
dc.publisherIMR Press Limited
dc.relation.ispartofClinical and Experimental Obstetrics and Gynecology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCarvacrol
dc.subjectInfertility
dc.subjectOxido-inflammatory
dc.subjectRat
dc.subject.classificationObstetrics & Gynecology
dc.subject.othercarvacrol
dc.subject.otherimmunoglobulin enhancer binding protein
dc.subject.otherinterleukin 1beta
dc.subject.otherprotein
dc.subject.othertumor necrosis factor
dc.subject.otheradult
dc.subject.otheranimal experiment
dc.subject.otheranimal model
dc.subject.otheranimal tissue
dc.subject.otherArticle
dc.subject.otherblood vessel
dc.subject.othercell infiltration
dc.subject.othercontrolled study
dc.subject.othercorpus luteum
dc.subject.otheredema
dc.subject.otherfemale
dc.subject.otherfemale infertility
dc.subject.otherhistopathology
dc.subject.otherinterstitium
dc.subject.otherleukocyte
dc.subject.othermale
dc.subject.othernonhuman
dc.subject.otherovary disease
dc.subject.otherovary tissue
dc.subject.otherrat
dc.subject.otherreperfusion injury
dc.titleThe effect of carvacrol on oxido-inflammatory ovarian injury and infertility induced by ischemia-reperfusion in rats
dc.typeArticle
rdl.citation.openalex2
rdl.citation.scopus2
rdl.citation.wos1
rdl.oa.statusgold
rdl.oa.urlhttps://www.imrpress.com/journal/CEOG/49/3/10.31083/j.ceog4903058/pdf
rdl.scopus.quartileQ4
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)